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Linda DeGraw

Associate Director, Contracts Specialist 

Linda has dedicated more than twenty-five years to drafting, negotiating and managing specialized contracts in the biopharmaceutical industry.

Her vast experience includes agreements for preclinical and clinical studies, research collaborations, master services and consulting, and other agreements relating to the development, manufacturing and testing of drug compounds. Linda contributes a valuable expertise to Faber, by focusing much of her work on clinical trial agreements for large multi-center studies, both in the U.S. and in other countries.

More about Linda

Consultant to Legal Division

Warner Chilcott (now Allergan)
  • Drafted and negotiated various agreements relating to the pharmaceutical industry

Manager, Pharmaceutical Licensing & Business Development

Warner-Lambert Company (now Pfizer)
  • Evaluated licensing opportunities
  • Assisted in structuring business deals
Legal Advisor, Corporate Legal Division
  • Responsible for a broad range of agreements relating to research and drug development activities

  • Phase 2/3 gene therapy clinical trial sponsored by bluebird bio, Inc.involving approximately 12 subjects across 5 sites in Europe and the US
  • Phase 3 clinical trial sponsored by BeiGene involving approximately 467 subjects across 150 sites in 20 countries located in Asia, Australia,Europe, Canada and the US
  • Phase 3 clinical trial sponsored by Tesaro, Inc. involving approximately 960 subjects across 225 sites in 25 countries located in Asia, Europe, Canada and the US

  • Model Agreements & Guidelines International (MAGI), member
  • Women in the Enterprise of Science & Technology (WEST), member

Interested in working with Linda?

Our team is eager to learn more about your project

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